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Travoprost Five Day Posology Study

Ocular Hypertension Clinical Trial

Clinical Trial Summary

The purpose of this study is to determine the safety and efficacy of three concentrations of travoprost ophthalmic solution (Groups A, B and C) administered eight times daily.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01114893
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase Phase 2
Start date April 2010
View Details
See also
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